Pro_Molecular_Structure:
pro_cdbregno:CCD00050135
枸橼酸奥芬那君
pro_formula:C18 H23 N O . C6 H8 O7
pro_molWeight:461.508
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| Product_Name： | 枸橼酸奥芬那君 |
| CAS： | 4682-36-4 ;4596-23-0 |
| 中文同义词： | 枸?酸?芬那君 ; 枸橼酸奥芬那君 |
| EnglishSynonyms： | BETA-DIMETHYLAMINOETHYL 2-METHYLBENZHYDRYL ETHER CITRATE SALT ; NORFLEX ; ORPHENADRINE CITRATE SALT ; 2-HYDROXYPROPANE-1,2,3-TRICARBOXYLIC ACID DIMETHYL((2-[(2-METHYLPHENYL)(PHENYL)METHOXY]ETHYL))AMINE ; MEPHENAMINE CITRATE ; O-METHYLDIPHENHYDRAMINE CITRATE SALT ; ORPHENADRINE CITRATE |
| pro_mdlNumber： | MFCD00079197 |
| pro_acceptors： | 2 |
| pro_donors： | 0 |
| pro_smile： | Cc1ccccc1C(c2ccccc2)OCCN(C)C.C(C(=O)O)C(CC(=O)O)(C(=O)O)O |
| InChi： | InChI=1S/C18H23NO.C6H8O7/c1-15-9-7-8-12-17(15)18(20-14-13-19(2)3)16-10-5-4-6-11-16;7-3(8)1-6(13,5(11)12)2-4(9)10/h4-12,18H,13-14H2,1-3H3;13H,1-2H2,(H,7,8)(H,9,10)(H,11,12) |
| InChiKey： | InChIKey=MMMNTDFSPSQXJP-UHFFFAOYSA-N |
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| Comments： | BIOCHEM/PHYSIOL ACTIONS: H1 HISTAMINE RECEPTOR ANTAGONIST BIOCHEM/PHYSIOL ACTIONS: MUSCARINIC RECEPTOR ANTAGONIST BIOCHEM/PHYSIOL ACTIONS: MUSCLE RELAXANT. ORPHENADRINE HAS ALSO BEEN REPORTED TO INHIBIT THE NORADRENERGIC TRANSPORTER AND TO BLOCK THE NMDA RECEPTOR ION CHANNEL STORAGE TEMPERATURE: 2-8 DEG C UNSPSC: 51000000 WGK: 3 |
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basic_info
* If the product has intellectual property rights, a license granted is must or contact us.
